Skyscape Web Viewer : International Classification of Diseases : ICD10 Index

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[E79.0]-Uricemia (asymptomatic)
[E79.1] - Lesch-Nyhan syndrome
[E79.1]-Lesch-Nyhan syndrome
[E79.2] - Myoadenylate deaminase deficiency
[E79.8] - Other disorders of purine and pyrimidine metabolism
[E79.81] - Aicardi-Goutières syndrome
[E79.82] - Hereditary xanthinuria
[E79.82]-Xanthinuria, hereditary
[E79.89] - Other specified disorders of purine and pyrimidine metabolism
[E79.9] - Disorder of purine and pyrimidine metabolism, unspecified
[E79] - Disorders of purine and pyrimidine metabolism
[E80.0] - Hereditary erythropoietic porphyria
[E80.0]-Protoporphyria, erythropoietic
[E80.1] - Porphyria cutanea tarda
[E80.2] - Other and unspecified porphyria
[E80.20] - Unspecified porphyria
[E80.21] - Acute intermittent (hepatic) porphyria
[E80.29]-Coproporphyria, hereditary
[E80.29] - Other porphyria
[E80.3]-Acatalasemia, acatalasia
[E80.3] - Defects of catalase and peroxidase
[E80.3]-Takahara's disease
[E80.4]-Bilirubinemia, familial nonhemolytic
[E80.4]-Gilbert's disease or syndrome
[E80.4] - Gilbert syndrome
[E80.5]-Crigler-Najjar disease or syndrome
[E80.5] - Crigler-Najjar syndrome
[E80.6]-Dubin-Johnson disease or syndrome
[E80.6] - Other disorders of bilirubin metabolism
[E80.6]-Rotor's disease or syndrome